Canonical Allele Identifier: CA2497327839

Gene: CCND1

Linked Data

• dbSNP Id: rs1590915468

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648236dup , CM000673.2:g.69648236dup	GRCh38
NC_000011.9:g.69463004dup , CM000673.1:g.69463004dup	GRCh37
NC_000011.8:g.69172185dup	NCBI36
NG_007375.1:g.12132dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+94dup MANE Select	ENSP00000227507.2:n.723+94dup
ENST00000227507.2:c.723+94dup	ENSP00000227507.2:n.723+94dup
ENST00000536559.1:c.*237dup	ENSP00000438482.1:n.*237dup
ENST00000542367.1:n.186+94dup
NM_053056.2:c.723+94dup	NP_444284.1:n.723+94dup
XM_006718653.2:c.747+94dup	XP_006718716.1:n.747+94dup
NM_053056.3:c.723+94dup MANE Select	NP_444284.1:n.723+94dup